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The Annals of Thoracic Surgery, Vol 58, 1368-1372, Copyright © 1994 by The Society of Thoracic Surgeons
SE Fremes, LR Guo, RD Furukawa, DA Mickle and RD Weisel
Previous investigations from our institution using an isolated human
cardiomyocyte model concluded that glucose supplementation of University of
Wisconsin solution (UWS) was beneficial with respect to adenine nucleotide
and protein recovery. We wished to confirm these results using an isolated
heart model. Rodent hearts were frozen in liquid nitrogen (control) or
flushed and stored in UWS for 8 hours at 0 degrees C or UWS supplemented
with 10, 20, or 30 mmol/L glucose. Experimental hearts were assessed at
end-storage or after 45 minutes of reperfusion on a Langendorff apparatus.
Adenine nucleotides were assessed by high performance liquid
chromatography. In parallel experiments, ventricular function was assessed
before and after storage in Langendorff-perfused hearts instrumented with a
left ventricular balloon. Glucose supplementation was associated with
greater poststorage (20 and 30 mmol/L glucose) and postreperfusion (10, 20,
and 30 mmol/L glucose) adenosine triphosphate levels than unmodified UWS.
Developed pressure (expressed as a percentage of control values) was
increased with 10 mmol/L glucose (75.2% +/- 7.9%, mean +/- standard
deviation) compared with unmodified UWS (64.6% +/- 6.6%; p < 0.05).
Coronary flow was greater with 10 (72.6% +/- 10.7%) or 20 mmol/L (71.2% +/-
12.5%) versus 0 mmol/L glucose (58.6% +/- 12.1%, p < 0.05). The data
support previous in vitro findings and suggest that the addition of 10
mmol/L glucose to UWS is associated with enhanced recovery after prolonged
hypothermic storage.
ARTICLES
Cardiac storage with UW solution and glucose
Division of Cardiovascular Surgery, University of Toronto, Ontario, Canada.
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